Linked Data
dbSNP Id:
rs1477759819
gnomAD v3:
6-35823412-C-CACAT
gnomAD v4:
6-35823412-C-CACAT
MyVariant Identifiers:
chr6:g.35791189_35791190insACAT (hg19)
chr6:g.35823412_35823413insACAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35823415_35823416insTACA , CM000668.2:g.35823415_35823416insTACA | GRCh38 |
| NC_000006.11:g.35791192_35791193insTACA , CM000668.1:g.35791192_35791193insTACA | GRCh37 |
| NC_000006.10:g.35899170_35899171insTACA | NCBI36 |
| NG_012184.1:g.23122_23123insTACA | |
| NG_012184.2:g.23122_23123insTACA | |
| NG_012184.3:g.31210_31211insTACA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360215.3:c.*450_*451insTACA MANE Select | ENSP00000353346.1:n.*450_*451insTACA | |
| ENST00000496656.2:n.578+3595_578+3596insTACA | ||
| ENST00000651132.1:c.*450_*451insTACA | ENSP00000498322.1:n.*450_*451insTACA | |
| ENST00000651676.1:c.*16+3952_*16+3953insTACA | ENSP00000498699.1:n.*16+3952_*16+3953insTACA | |
| ENST00000651994.1:c.*530_*531insTACA | ENSP00000498310.1:n.*530_*531insTACA | |
| ENST00000652718.1:c.508+3952_508+3953insTACA | ENSP00000498866.1:n.508+3952_508+3953insTACA | |
| ENST00000360215.2:c.*450_*451insTACA | ENSP00000353346.1:n.*450_*451insTACA | |
| ENST00000496656.1:n.812+3595_812+3596insTACA | ||
| NM_182548.3:c.*450_*451insTACA | NP_872354.1:n.*450_*451insTACA | |
| NM_182548.4:c.*450_*451insTACA MANE Select | NP_872354.1:n.*450_*451insTACA |